4.7 Article

Absence of Association Between the INSIG2 Gene Polymorphism (rs7566605) and Obesity in the European Youth Heart Study (EYHS)

期刊

OBESITY
卷 17, 期 7, 页码 1453-1457

出版社

WILEY
DOI: 10.1038/oby.2008.650

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资金

  1. The Danish Heart Foundation
  2. The Danish Medical Research Council Health Foundation
  3. The Danish Council for Sports Research
  4. The Foundation in Memory of Asta Florida Bolding Renee Andersen
  5. The Faculty of Health Sciences
  6. University of Southern Denmark
  7. The Estonian Science Foundation [3277, 5209]
  8. Novo Nordisk [370579201]
  9. Swedish Diabetes Association [DIA2006-013]
  10. MRC [MC_U106179473, MC_U106188470] Funding Source: UKRI
  11. Medical Research Council [MC_U106179471, MC_U106188470, MC_U106179473] Funding Source: researchfish

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The first genome-wide association study for BMI identified a polymorphism, rs7566605, 10 kb upstream of the insulin-induced gene 2 (INSIG2) transcription start site, as the most significantly associated variant in children and adults. Subsequent studies, however, showed inconsistent association of this polymorphism with obesity traits. This polymorphism has been hypothesized to alter INSIG2 expression leading to inhibition of fatty acid and cholesterol synthesis. Hence, we investigated the association of the INSIG2 rs7566605 polymorphism with obesity-and lipid-related traits in Danish and Estonian children (930 boys and 1,073 girls) from the European Youth Heart Study (EYHS), a school-based, cross-sectional study of pre- and early pubertal children. The association between the polymorphism and obesity traits was tested using additive and recessive models adjusted for age, age-group, gender, maturity and country. Interactions were tested by including the interaction terms in the model. Despite having sufficient power (98%) to detect the previously reported effect size for association with BMI, we did not find significant effects of rs7566605 on BMI (additive, P = 0.68; recessive, P = 0.24). Accordingly, the polymorphism was not associated with overweight (P = 0.87) or obesity (P = 0.34). We also did not find association with waist circumference (WC), sum of four skinfolds, or with total cholesterol, triglycerides, low-density lipoprotein, or high-density lipoprotein. There were no gender-specific ( P = 0.55), age-group-specific (P = 0.63) or country-specific (P = 0.56) effects. There was also no evidence of interaction between genotype and physical activity (P = 0.95). Despite an adequately powered study, our findings suggest that rs7566605 is not associated with obesity-related traits and lipids in the EYHS.

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